Seuraa
khalid Hussain
khalid Hussain
Sidra Medicine
Vahvistettu sähköpostiosoite verkkotunnuksessa sidra.org
Nimike
Viittaukset
Viittaukset
Vuosi
Recommendations from the pediatric endocrine society for evaluation and management of persistent hypoglycemia in neonates, infants, and children
PS Thornton, CA Stanley, DD De Leon, D Harris, MW Haymond, ...
The Journal of pediatrics 167 (2), 238-245, 2015
6042015
Insulin Mutation Screening in 1,044 Patients With Diabetes: Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes …
EL Edghill, SE Flanagan, AM Patch, C Boustred, A Parrish, B Shields, ...
Diabetes 57 (4), 1034-1042, 2008
4762008
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency
RS Jackson, JWM Creemers, IS Farooqi, ML Raffin-Sanson, A Varro, ...
The Journal of clinical investigation 112 (10), 1550-1560, 2003
4122003
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
F Brioude, JM Kalish, A Mussa, AC Foster, J Bliek, GB Ferrero, ...
Nat Rev Endocrinol 14 (4), 229-249, 2018
3922018
Practical management of hyperinsulinism in infancy
A Aynsley-Green, K Hussain, J Hall, JM Saudubray, C Nihoul-Fekete, ...
Archives of Disease in Childhood-Fetal and Neonatal Edition 82 (2), F98-F107, 2000
3732000
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion
PT Clayton, S Eaton, A Aynsley-Green, M Edginton, K Hussain, ...
The Journal of clinical investigation 108 (3), 457-465, 2001
3702001
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
M Bitner-Glindzicz, KJ Lindley, P Rutland, D Blaydon, VV Smith, PJ Milla, ...
Nature genetics 26 (1), 56-60, 2000
3692000
Noninvasive Diagnosis of Focal Hyperinsulinism of Infancy With [18F]-DOPA Positron Emission Tomography
T Otonkoski, K Näntö-Salonen, M Seppänen, R Veijola, H Huopio, ...
Diabetes 55 (1), 13-18, 2006
3172006
Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis
MN Weedon, I Cebola, AM Patch, SE Flanagan, E De Franco, R Caswell, ...
Nature genetics 46 (1), 61-64, 2014
3082014
What is a normal blood glucose?
M Güemes, SA Rahman, K Hussain
Archives of disease in childhood 101 (6), 569-574, 2016
2932016
Re-evaluating “transitional neonatal hypoglycemia”: mechanism and implications for management
CA Stanley, PJ Rozance, PS Thornton, DD De Leon, D Harris, ...
The Journal of pediatrics 166 (6), 1520-1525. e1, 2015
2772015
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism
RR Kapoor, SE Flanagan, VB Arya, JP Shield, S Ellard, K Hussain
European journal of endocrinology 168 (4), 557-564, 2013
2532013
The genetic basis of congenital hyperinsulinism
C James, RR Kapoor, D Ismail, K Hussain
Journal of medical genetics 46 (5), 289-299, 2009
2282009
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis
I Garin, EL Edghill, I Akerman, O Rubio-Cabezas, I Rica, JM Locke, ...
Proceedings of the National Academy of Sciences 107 (7), 3105-3110, 2010
2192010
An activating mutation of AKT2 and human hypoglycemia
K Hussain, B Challis, N Rocha, F Payne, M Minic, A Thompson, A Daly, ...
Science 334 (6055), 474-474, 2011
1962011
Hyperinsulinaemic hypoglycaemia
RR Kapoor, SE Flanagan, C James, J Shield, S Ellard, K Hussain
Archives of Disease in Childhood 94 (6), 450-457, 2009
1862009
Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management
S Senniappan, B Shanti, C James, K Hussain
Journal of inherited metabolic disease 35, 589-601, 2012
1802012
Diagnosis and management of hyperinsulinaemic hypoglycaemia of infancy
K Hussain
Hormone Research in Paediatrics 69 (1), 2-13, 2007
1692007
Congenital hyperinsulinism: diagnosis and treatment update
H Demirbilek, K Hussain
Journal of clinical research in pediatric endocrinology 9 (Suppl 2), 69, 2017
1662017
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man
SE Flanagan, E De Franco, HL Allen, M Zerah, MM Abdul-Rasoul, ...
Cell metabolism 19 (1), 146-154, 2014
1662014
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Artikkelit 1–20